Homo sapiens (human): 645104 Help Entry 645104            CDS       T01001                                  Symbol CLRN2, DFNB117 Name (RefSeq) clarin 2   KO K23841   clarin Organism hsa  Homo sapiens (human) Disease H00605   Deafness, autosomal recessive Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:hsa03037]     645104 (CLRN2) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   USH complex and associated proteins    645104 (CLRN2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PMP22_Claudin Motif Other DBs NCBI-GeneID:  645104 NCBI-ProteinID:  NP_001073296 OMIM:  618988 HGNC:  33939 Ensembl:  ENSG00000249581 UniProt:  A0PK11 LinkDB All DBs Position 4:17515165..17527104 Genome browser AA seq 232 aa AA seqDB search MPGWFKKAWYGLASLLSFSSFILIIVALVVPHWLSGKILCQTGVDLVNATDRELVKFIGD IYYGLFRGCKVRQCGLGGRQSQFTIFPHLVKELNAGLHVMILLLLFLALALALVSMGFAI LNMIQVPYRAVSGPGGICLWNVLAGGVVALAIASFVAAVKFHDLTERIANFQEKLFQFVV VEEQYEESFWICVASASAHAANLVVVAISQIPLPEIKTKIEEATVTAEDILY NT seq 699 nt NT seq  +upstreamnt  +downstreamnt atgcctggatggttcaaaaaggcgtggtatgggctggcgtctttactcagcttctcctcc ttcatcctgatcatcgttgccctggtagtgccccactggctgagtgggaaaatcctttgt cagactggagtggatctggtcaacgccacagacagagagctggtcaagttcattggggac atttactacgggctcttccgagggtgtaaagtgcggcagtgtgggcttgggggccgccaa tcccaattcacgatcttcccacacctggtgaaggagctcaacgcaggccttcatgtgatg attctgctgctcctcttcctggccttggccctggctctggtcagcatgggctttgccatt cttaacatgatccaggtcccgtaccgggcagtcagcggtcctgggggcatctgcctatgg aatgtcctggcaggcggcgtcgtggcgttagccatcgccagcttcgtggctgcggtgaaa tttcacgacctgacggaacgaatcgccaactttcaggagaagctcttccagtttgtggtg gtggaagaacagtatgaagagtcgttttggatctgcgtggccagcgcttcggcccatgct gcaaacttggtcgtggtggcgatcagtcaaattcccctccctgagattaagaccaaaatc gaagaggccacggtcacagctgaggatatcttgtattaa

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